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. Author manuscript; available in PMC: 2014 Jan 1.
Published in final edited form as: Behav Genet. 2012 Dec 21;43(1):60–70. doi: 10.1007/s10519-012-9574-6

Fig. 4.

Fig. 4

A schematic diagram and results from fluorescence in situ hybridization showing the locations of zebra finch BAC clones 5K13 (red) and 55A1 (green) on ZAL2 and ZAL2m. The two clones hybridize close together on the long arm of ZAL2, but because of an inversion, they map to opposite arms of ZAL2m (a). Tan-striped (TS) birds have two copies of ZAL2 (b) and white-striped (WS) birds have one copy of ZAL2 and one of ZAL2m (c). Bird 1128 clearly shows the ZAL2m hybridization pattern on two chromosomes (d). The chromosome map in (a) shows the locations of the three markers used to genotype Bird 1128 via PCR